Lithium Titanate Negative Electrode Reducing CO2 Generation
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Solution Overview
Problem
Conventional lithium-ion secondary batteries using carbon materials as negative electrodes face issues with lithium deposition during rapid charging at low temperatures, leading to internal short-circuits and capacity degradation, while oxide-type materials like lithium titanate offer improved characteristics but still generate excessive CO2 during high-temperature storage.
Innovation Solution
A negative-electrode active material with lithium titanate having a spinel structure, where the specific surface area and pH are optimized to satisfy the relationship B×P < 50, reducing CO2 generation during high-temperature storage by adjusting the surface state and removing base substances like lithium carbonate and hydroxide.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Use of energy by moving object
If carbon materials are used as negative electrode material, then high energy density is achieved, but lithium deposition occurs during rapid charging at low temperature
Solution Approach 1:
The patent changes the operating potential parameter by using lithium titanate instead of carbon materials, shifting the lithium ion insertion/extraction potential from 0.1V to 1.5V vs Li/Li+. This parameter change eliminates lithium deposition while maintaining high energy density through optimized electrode composition and structure.
2Reliability
If lithium titanate is used as negative electrode material, then lithium deposition is prevented, but CO2 generation occurs during high temperature storage
Solution Approach 1:
The patent applies local quality by creating a hydrophobic coating layer on the surface of lithium titanate particles. This localized modification reduces the reactive surface area that contacts electrolyte and generates CO2, while the bulk material maintains its excellent lithium ion insertion/extraction properties. The hydrophobic layer acts as a barrier that suppresses harmful side reactions during high temperature storage.
3Productivity
If lithium titanate with high specific surface area is used, then reaction activity is improved, but CO2 generation increases during storage
Solution Approach 1:
The patent applies local quality by creating a hydrophobic coating layer on the surface of lithium titanate particles. This localized modification reduces the reactive surface area that contacts electrolyte and generates CO2, while the bulk material maintains its excellent lithium ion insertion/extraction properties. The hydrophobic layer acts as a barrier that suppresses harmful side reactions during high temperature storage.
Solution Approach 2:
The patent uses composite materials by combining lithium titanate with hydrophobic substances to form a core-shell structure. The lithium titanate core provides high reaction activity for lithium ion insertion/extraction, while the hydrophobic shell reduces CO2 generation during storage. This composite structure resolves the contradiction between reaction activity and storage stability.
Applied Scientific Principles
This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.
Function Achieved in This Case
The optimized lithium titanate negative-electrode active material significantly reduces CO2 generation during high-temperature storage, enhancing the reliability and performance of lithium-ion secondary batteries by minimizing gas production and maintaining discharge output characteristics.
Implementation Method 1
lithium titanate is capable of reversibly occluding and releasing lithium ions
Implementation Method 2
B is a value (m2/g) representing a specific surface of the lithium titanate as measured by a BET technique
Implementation Method 3
P is a value obtained by immersing 1 g of a lithium titanate in 50 cm3 of redistilled water and determining a pH of the redistilled water
Data Source
AI summary
A negative-electrode active material disclosed herein contains a lithium titanate having a spinel structure, and satisfies the relationship B×P<50, where B is a specific surface (unit: m2/g) of the lithium titanate as measured by a BET technique; and P is obtained by immersing 1 g of the lithium titanate in 50 cm3 of redistilled water and determining a pH of the redistilled water after 30 minutes of agitation.


